ERK/MAPK Pathway Inhibitor Development

ERK/MAPK Pathway Inhibitor Development

In the context of breast cancer, dysregulation of ERK/MAPK pathway can lead to uncontrolled cell growth, increased metastatic potential, and resistance to conventional therapies. At Alfa Cytology, we specialize in unraveling the intricacies of the ERK/MAPK pathway and developing of new ERK/MAPK pathway inhibitor for breast cancer therapy.

Introduction to ERK/MAPK Pathway Inhibitor for Breast Cancer

The ERK/MAPK pathway is a fundamental signaling cascade that integrates extracellular signals, such as growth factors and cytokines, and transduces them into intracellular responses. In the context of breast cancer, dysregulation of this pathway can lead to the hallmarks of this malignancy, including uncontrolled cell proliferation, evasion of apoptosis, and increased migratory and invasive capabilities.

Fig.1 Angiogenesis and tumor vasculature. (Ayoub N. M., et al. 2022)Fig.1 Schematic overview of the Ras/MAPK signaling pathway. (Giltnane J. M., et al. 2014)

At the core of this signaling network are the Ras, Raf, MEK, and ERK proteins, which form a highly orchestrated cascade of phosphorylation events. Alterations in the activity or expression of these key components can disrupt the delicate balance of cellular processes, ultimately contributing to the initiation and progression of breast cancer.

ERK/MAPK Pathway Inhibitor Development for Breast Cancer

The ERK/MAPK (extracellular signal-regulated kinase/mitogen-activated protein kinase) signaling pathway is a critical target for the development of novel breast cancer therapies. Several types of ERK/MAPK pathway inhibitors are being explored for the treatment of breast cancer, each with its own unique mechanism of action and potential therapeutic applications.

NCT number Target Therapeutic Phase
NCT02322853 p38 MAPK LY2228820 dimesylate
NCT01155453 MEK GSK1120212
NCT06239623 MAPK Signaling Pathway JSI-1187
NCT06287463 MAPK Pathway DCC-3084
NCT06299839 MEK (1/2) PAS-004
NCT04249843 RAF BGB-3245

Our Services

Recognizing the pivotal role of the ERK/MAPK pathway in breast cancer, the researchers at Alfa Cytology have dedicated their efforts to the development of targeted inhibitors that can disrupt this critical signaling axis. By selectively targeting key components within the pathway, such as Raf kinases, MEK, and ERK, our team aims to design novel therapeutic strategies that can effectively combat breast cancer.

Raf Kinase Inhibitor Development

  • Novel pan-RAF Inhibitor Development
  • RAF Dimer Inhibitor Development

MEK Inhibitor Development

  • Allosteric MEK Inhibitor Development
  • Dual MEK/ERK Inhibitor Development

ERK Inhibitor Development

  • ATP-Competitive ERK Inhibitor Development
  • Allosteric ERK Inhibitor Development
  • Covalent ERK Inhibitor Development

Our Therapeutics Development Platform for ERK/MAPK Pathway Inhibitor Development

At Alfa Cytology, we pride ourselves on our comprehensive suite of preclinical services tailored to the development of innovative ERK/MAPK pathway inhibitors for breast cancer. We are committed to driving the development of transformative E Platform RK/MAPK pathway inhibitors that have the potential to revolutionize the treatment of breast cancer. To learn more about our capabilities in ERK/MAPK pathway inhibitor development for breast cancer or to discuss potential collaborative opportunities, please don't hesitate to contact us.

Reference

  1. Giltnane J. M., Balko J. M. Rationale for targeting the Ras/MAPK pathway in triple-negative breast cancer. Discov Med. 2014, 7(95): 275-83.
All our services are exclusively intended for preclinical research purposes. They are not intended for diagnostic, therapeutic, or patient management applications.
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